Molecular simulation of HER2/neu degradation by inhibiting HSP90

作者：Chen Calvin Yu Chian; Chen Guan Wen; Chen Winston Yu Chen

来源：Journal of the Chinese Chemical Society, 2008, 55(2): 297-302.

DOI：10.1002/jccs.200800044

• HSP90
• HER2/neu (ErbB-2)
• luteolin
• docking
• molecular simulation
• flavonoid
• 1-benzyl-3-(5-hydroxymethyl-2-furyl)indazole (YC-1)

Several flavonoids were investigated for the degradation of the HER2/neu (ErbB-2), while the mechanism is still unknown. A hypothesis was generated here that the inhibition of HER2/neu expression was blocked by heat shock protein 90 alpha (HSP90 alpha) through 1-benzyl-3-(5-hydroxymethyl-2-furyl)indazole (YC-1) derivatives and flavonoids. In order to ensure the accuracy of the simulated protein structure, the RMSD value between the ligand in crystal structure from PDB and the ligand docking into HSP90 alpha was 1.13 angstrom. By molecular simulation, the flavonoids and YC-1 derivatives were employed to dock into HSP90 alpha. The results showed a good correlation between the evaluation scores of the flavonoids/HSP90 alpha complexes and the IC50 of flavonoids-induced degradation of HER2/neu. The YC-1 derivatives showed higher score values and lower interaction energies on average. Especially, the CLC107 got the highest rank in Potential of Mean Force (PMF) and Dock Score. Luteolin showed the highest dock score and quercetin had the lowest interaction energy of all flavonoid derivatives. This study investigated that the YC-1 derivatives and the flavonoids may be potent inhibitors for HSP90 alpha in antitumor strategies.

• 出版日期2008-4
• 单位中国医科大学